Axsym Carbamazephine

FDA 510(k) K935374 · Abbott Laboratories

Substantially Equivalent

510(k) numberK935374

Submission

Device name
Axsym Carbamazephine
Applicant
Abbott Laboratories
Abbott Park, IL, US
Received
November 8, 1993
Decision date
June 21, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KLT – Enzyme Immunoassay, Carbamazepine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3645
Specialty
Clinical Toxicology

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K010814Emit 2000 Carbamazepine Assay, Model OSR4F229KLT · Special Syva Co., Dade Behring, Inc.04/13/2001SE
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K000007Immulite Carbamazepine, Immulite 2000 Carbamazepine, Catalog # LKCB1, LKCB5 & L2KCB2…KLT · Traditional Diagnostic Products Corp.02/28/2000SE

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Questions and answers

When was Axsym Carbamazephine cleared by the FDA?

Axsym Carbamazephine (K935374) received a 510(k) decision of Substantially Equivalent on June 21, 1994, 225 days after the submission was received.

What is the product code of K935374?

The FDA product code is KLT – Enzyme Immunoassay, Carbamazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3645.